![PDF] The role of contactin-associated protein-like 2 in neurodevelopmental disease and human cerebral cortex evolution](https://www.researchgate.net/publication/364473606/figure/fig1/AS:11431281091285061@1666364690604/Location-and-structure-of-the-contactin-associated-protein-like-2-CNTNAP2-gene-and_Q320.jpg "PDF] The role of contactin-associated protein-like 2 in neurodevelopmental disease and human cerebral cortex evolution")
PDF] The role of contactin-associated protein-like 2 in neurodevelopmental disease and human cerebral cortex evolution
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | PLOS Genetics
CNTNAP2 Heterozygous Missense Variants: Risk Factors for Autism Spectrum Disorder and/or Other Pathologies? - Giorgia Canali, Laurence Goutebroze, 2018
Genetics of structural and functional brain changes in autism spectrum disorder | Translational Psychiatry
Expanding the clinical spectrum associated with defects in CNTNAP2 and NRXN1 | BMC Medical Genetics | Full Text
Publications of the week – CNTNAP2, DEPDC5, and autism whole-genome sequencing | Beyond the Ion Channel
Characterisation of CASPR2 deficiency disorder - a syndrome involving autism, epilepsy and language impairment | BMC Medical Genetics | Full Text
Altered cingulate structures and the associations with social awareness deficits and CNTNAP2 gene in autism spectrum disorder - ScienceDirect
Transcriptional regulation network of CNTNAP2 (A) and the Caspr2... | Download Scientific Diagram
Contactinâ•'associated proteinâ•'like 2, a protein of the neurexin family involved in several human diseases
Linking neuroanatomical abnormalities in autism spectrum disorder with gene expression of candidate ASD genes: A meta-analytic and network-oriented approach | PLOS ONE
Shining a light on CNTNAP2: complex functions to complex disorders | European Journal of Human Genetics
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | PLOS Genetics
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text
Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | Molecular Psychiatry
CNTNAP2 Mutations in Autism - ScienceDirect
Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | Molecular Psychiatry
Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | Molecular Psychiatry
What does CNTNAP2 reveal about autism spectrum disorder? - ScienceDirect
Frontiers | Using Zebrafish to Model Autism Spectrum Disorder: A Comparison of ASD Risk Genes Between Zebrafish and Their Mammalian Counterparts
Cntnap2-dependent molecular networks in autism spectrum disorder revealed through an integrative multi-omics analysis | Molecular Psychiatry
Role of CNTNAP2 in autism manifestation outlines the regulation of signaling between neurons at the synapse | Egyptian Journal of Medical Human Genetics | Full Text
JCM | Free Full-Text | Altered Blood Brain Barrier Permeability and Oxidative Stress in Cntnap2 Knockout Rat Model
Location of all mutations of interest, i.e. rare and exclusive to cases... | Download Scientific Diagram
Comprehensive cross-disorder analyses of CNTNAP2 suggest it is unlikely to be a primary risk gene for psychiatric disorders | PLOS Genetics
